Page 33 - Handbook of Adhesion Promoters
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26                                                  Mechanisms of Adhesion


                        46
            polymerization.  The twin polymerization was performed using the following monomers:
            2,20-spirobi-[4H-1,3,2-benzodioxasiline]  and  2-(3-amino-n-propyl)-2-methyl-4H-1,3,2-
                          46
            benzodioxasiline.   The  resultant  polymer  is  very  convenient  for  use  as  an  interphase
            because it is produced without shrinkage and formation of low-molecular weight prod-
                46
            ucts.
                Resist lithography is used in the electronics industry as a common microfabrication
                    47
            technique.  Epoxy oligomer (SU 8) is a favorite photoresist material but it suffers from
                                                               47
            poor adhesion to silicon which is used as the common substrate.  A layer of polyallylam-
            ine was found to be an excellent adhesion promoter because it spontaneously absorbs on
                                                            47
            silicon and has amine groups reactive with epoxy oligomer.  Figure 2.24 shows steps of
                          47
            microfabrication.
                                                            Figure 2.25 shows a method
                                                        of  fabrication  of  a  digital  micro-
                                                        fluidic chip from poly(p-xylylene)
                                                        (Parylene C) and tantalum pentox-
                                                           48
                                                        ide.  Because both layers do not
                                                        have sufficient adhesion, the inter-
                                                        mediate layer has to be produced
                                                                          48
                                                        to hold them together.  This layer
                                                        is  formed  from  γ-methacryloxy-
                                                                            48
                                                        propyltrimethoxy silane.  During
                                                        the coating process, the surface of
                                                        Ta O  reacts with adsorbed water
                                                            5
                                                          2
                                                        molecules  in  the  air  and  forms  a
                                                                              48
                                                        hydroxyl  group,  Ta−OH.  The
                                                        hydroxyl group reacts with silane
                                                        forming  a  self-limited  molecular
                                                        layer on the Ta O  surface (Figure
                                                                    2
                                                                      5
                                                              48
                                                        2.25c).    The   monomers   of
                                                        Parylene  C  deposited  on  the  sur-
                                                        face of a polymerized silane (Fig-
                                                        ure  2.25b) copolymerize with  the
                                                        methacryloxy tail via a free radical
                                                        addition reaction and deposit as a
                                                                    48
                                                        polymer  layer.   This  technology
                                                        leads to the formation of very thin
                                                        (monomolecular)      interface
                                                                        48
                                                        enhancing adhesion.
                                                            Figure 2.26 shows the struc-
                                                        ture  of  electrode  material  com-
            Figure 2.26. (a) Cross-sectional image of film without (3-glyci-
            doxypropyl) trimethoxysilane prepolymer and (b) film with 1.0   posed  of  polyimide  and  copper
                                                            49
            wt% (3-glycidoxypropyl) trimethoxysilane prepolymer on polyim-  paste.   The  copper  paste  is
                              o
            ide substrate sintered at 275 C in nitrogen/HCOOH environment.   applied on the surface of polyim-
            [Adapted, by permission, from Jiang, J; Koo, YH; Kim, HW; Park,
            JH; Kang, HS; Lee, BC; Kim, S-H; Song, H-e; Piao, L, Bull.   ide  core  with  1  wt%  of  3-glyci-
            Korean Chem. Soc., 35, 10, 3025-9, 2014.]   doxypropyltrimethoxysilane
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